Canonical Allele Identifier: CA3854347
Gene: IL17F HGNC NCBI

Linked Data

ClinVar Variation Id: 357468
dbSNP Id: rs11465553
gnomAD v2: 6-52101758-C-T
gnomAD v3: 6-52236960-C-T
gnomAD v4: 6-52236960-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52236960C>T , CM000668.2:g.52236960C>T GRCh38
NC_000006.11:g.52101758C>T , CM000668.1:g.52101758C>T GRCh37
NC_000006.10:g.52209717C>T NCBI36
NG_031869.1:g.12541G>A , LRG_356:g.12541G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000699946.1:c.463G>A ENSP00000514702.1:p.Val155Ile
ENST00000336123.5:c.463G>A MANE Select ENSP00000337432.4:p.Val155Ile
ENST00000336123.4:c.463G>A ENSP00000337432.4:p.Val155Ile
ENST00000478427.1:n.647G>A
NM_052872.3:c.463G>A , LRG_356t1:c.463G>A NP_443104.1:p.Val155Ile
XM_011514276.1:c.463G>A XP_011512578.1:p.Val155Ile
NM_052872.4:c.463G>A MANE Select NP_443104.1:p.Val155Ile